Canonical Allele Identifier: CA2275256792
Gene: USH1G HGNC NCBI

Linked Data

dbSNP Id: rs2038961268

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74922832G>A , CM000679.2:g.74922832G>A GRCh38
NC_000017.10:g.72918927G>A , CM000679.1:g.72918927G>A GRCh37
NC_000017.9:g.70430522G>A NCBI36
NG_007882.1:g.5425C>T
NG_033062.1:g.3558G>A
NG_007882.2:g.5432C>T
NG_033062.2:g.3558G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000614341.5:c.164+78C>T MANE Select ENSP00000480279.1:n.164+78C>T
ENST00000579243.1:c.164+78C>T ENSP00000462568.1:n.164+78C>T
ENST00000614341.4:c.164+78C>T ENSP00000480279.1:n.164+78C>T
NM_001282489.2:c.-93+78C>T NP_001269418.1:n.-93+78C>T
NM_173477.4:c.164+78C>T NP_775748.2:n.164+78C>T
XM_011524296.1:c.-402C>T XP_011522598.1:n.-402C>T
XM_011524296.2:c.-402C>T XP_011522598.1:n.-402C>T
NM_173477.5:c.164+78C>T MANE Select NP_775748.2:n.164+78C>T
NM_001282489.3:c.-93+78C>T NP_001269418.1:n.-93+78C>T